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Trial record 1 of 1 for:    NCT04054375
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Weekly Steroids in Muscular Dystrophy (WSiMD)

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ClinicalTrials.gov Identifier: NCT04054375
Recruitment Status : Completed
First Posted : August 13, 2019
Results First Posted : July 8, 2021
Last Update Posted : February 16, 2023
Information provided by (Responsible Party):
Senda Ajroud-Driss, Northwestern University

Brief Summary:

The purpose of this study is to evaluate the safety and efficacy of oral weekly glucocorticoid steroids in patients with Becker Muscular Dystrophy (BMD), an inherited disorder in which patients experience weakness of the legs and pelvis, and Limb Girdle Muscular Dystrophy (LGMD), an inherited disorder in which patients experience progressive muscular weakness predominately in their hip and shoulders. The primary objective is safety which we the investigators will measure using laboratory testing and forced vital capacity (FVC), a breathing test that measures the strength of your lungs. The secondary objective is efficacy which will be measured by a change in MRI muscle mass, improved muscle performance, and quality of life.

The investigators hypothesize that patients who receive oral weekly glucocorticoid steroids will have improviements in strength and quality of life compared to their baseline. Furthermore, the investigators anticipate that oral weekly glucocorticoid steroids will not have significant adverse impact on patients.

Condition or disease Intervention/treatment Phase
Limb-girdle Muscular Dystrophy Becker Muscular Dystrophy Drug: Prednisone Phase 2

Detailed Description:

Glucocorticoid (GC) steroids are a mainstay of therapy for Duchenne Muscular Dystrophy, where they have been shown to prolong ambulation in for DMD in random clinical trials (Gloss et al., 2016). Dosing regimen vary for DMD, but most trials utilized oral daily dosing at 0.75- 1 mg/kg of prednisone or deflazacort (Birnkrant et al., 2018). The age at which to begin oral glucocorticoids and the age at which to cease steroid use are not well established by clinical trial investigation. High dose weekend dosing of oral glucocorticoid steroids has also been suggested to be noninferior to daily dosing when evaluated in a year-long study in DMD, and this approach is preferred in some settings since related to a reduced side effect profile, particularly with respect to behavioral changes which can occur with daily GC steroid dosing in children (Escolar et al., 2011). The use of GC steroids for other forms of muscular dystrophy, including Becker Muscular Dystrophy (BMD) and the Limb Girdle Muscular Dystrophies (LGMDs) is not considered standard of care and has insufficiently been investigated by randomized clinical trials (RCT). An RCT of GC steroids in LGMD 2B (DYSF mutations) was associated with unfavorable outcomes in the steroid treated group (Walter et al., 2013).

Recently, weekly steroid dosing was investigated in preclinical mouse models of muscular dystrophy, including the mdx mouse model of DMD/BMD and two models of LGMD, including LGMD 2B (DYSF) and 2C (SGCG) (Quattrocelli et al., 2017a; Quattrocelli et al., 2017b). All three models showed improved strength and reduced fibrosis with weekly GC steroid dosing. Moreover, in unpublished data, long term studies (24-52 weeks duration) in mice, showed favorable results with improved muscle strength in the mdx and DYSF models.

The investigators propose to carry out an open label safety and efficacy trial of oral weekly GC steroids in patients with BMD and LGMD subtypes. Subjects will be recruited based on age, molecular diagnosis of BMD and LGMD subtypes, and willingness to participate. Both ambulatory and nonambulatory subjects will be included. Subjects will be excluded if they have diabetes mellitus, full time ventilator use, or severely compromised cardiac function, including symptoms referable to heart failure. Subjects must provide consent.

Subjects will be asked to take weekly GC oral prednisone dosed based on weight (1mg/kg for patients who weigh less than or equal to 70 kg and 0.75 mg/kg for patients who weigh more than 70 kg). Subjects will also be instructed to take their weekly prednisone on Mondays after their last meal between 7 and 9 PM. Prior to initiation, subjects will provide a blood sample for baseline screening including serum chemistries, HgbA1-C, creatine kinase, and lipid panel (HDL, LDL, triglycerides, and total cholesterol) and for exploratory biomarkers. Subjects will also provide a urine sample to analyze changes in metabolic biomarkers that are excreted. Subjects will have a physical exam and medical record review. Subjects will have strength testing and complete 10 meter timed run test in addition to a 6 min walk test (if ambulatory). Subjects will be asked to complete quality of life questionnaire. At 6 months, subjects will be evaluated with a physical exam, strength testing, spirometry, 10 meter timed run test and 6 min walk test (if ambulatory), blood draw for serum chemistry, HgbA1-C, creatine kinase, lipid panel and for exploratory biomarkers. Subjects will also provide a urine specimen to be analyzed for any changes in excretion of metabolic markers as an exploratory endpoint. Subjects will be asked to complete a quality of life questionnaire. An MRI/ MRS will be performed before starting GC oral prednisone and at 6 months.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 20 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Open Label Safety and Efficacy of Once Weekly Steroid in Patients With LGMD and Becker Muscular Dystrophy
Actual Study Start Date : July 1, 2019
Actual Primary Completion Date : June 1, 2020
Actual Study Completion Date : March 1, 2022

Arm Intervention/treatment
Experimental: Weekly Steroid
Subjects will be asked to take weekly GC oral prednisone dosed based on weight (1mg/kg for patients who weigh less than or equal to 70 kg and 0.75 mg/kg for patients who weigh more than 70 kg). Subjects will also be instructed to take their weekly prednisone on Mondays after their last meal between 7 and 9 PM
Drug: Prednisone
Subjects will be asked to take weekly GC oral prednisone dosed based on weight (1mg/kg for patients who weigh less than or equal to 70 kg and 0.75 mg/kg for patients who weigh more than 70 kg). Subjects will also be instructed to take their weekly prednisone on Mondays after their last meal between 7 and 9 PM
Other Name: Prednisolone

Primary Outcome Measures :
  1. Fasting Glucose [ Time Frame: Baseline and 6 months (Final Visit) ]
    mg/dL, 0-unlimited, higher score indicates worse outcome

  2. HbgA1c [ Time Frame: Baseline and 6 months (Final Visit) ]
    % , 0-100, higher score indicates worse outcome

  3. Fasting Lipid Profile [ Time Frame: Baseline and 6 months (Final Visit) ]
    cholesterol levels - mg/dL, higher levels indicate worse outcomes

  4. Creatine Kinase [ Time Frame: Baseline and 6 months (Final Visit) ]
    units/L, 0-unlimited, higher scores indicate worse outcome

  5. Respiratory Changes [ Time Frame: Baseline, 6 months ]
    Force Vital Capacity (% of predicted value), decrease in FVC indicates declining respiratory function.

Secondary Outcome Measures :
  1. Functional Assessments - NSAD Change [ Time Frame: Baseline, Month 6 ]

    Northstar Assessment for Dysferlinopathy

    - score out of 58, range from 0 to 58, higher score indicates greater functional ability.

  2. 6 Minute Walk Test [ Time Frame: Baseline, Month 6 ]
    number of meters walked in 6 minute period. Higher values indicate more motor function.

  3. 10 Meter Run Timed [ Time Frame: Baseline, Month 6 ]
    time in seconds to walk/run 10 meters , less time to run indicates greater motor function

  4. Functional Assessments - Upper Limb Strength [ Time Frame: Baseline, Month 6 ]
    Performance of Modified Upper Limb Module - Yes or No questions, ability to raise 50 gram, 100 gram, 200 gram, 500 gm weights above the head and to the mouth.

  5. Brooke Scale Score [ Time Frame: Baseline, Month 6 ]
    upper extremity assessment, scoring between 1- 6, lower score indicates more upper extremity function

  6. Vignos Scale Score [ Time Frame: Baseline, Month 6 ]
    Lower extremity assessment, score from 1-10, lower score indicates more function.

  7. Muscle Strength Test [ Time Frame: Baseline, 6 months ]
    Motor Muscle Testing: score of 1 - 5 , higher score indicates more muscle strength.

  8. Muscle Imaging [ Time Frame: Baseline, 6 months ]
    MRI of leg muscles to measure changes in muscle

  9. Bone Density [ Time Frame: Baseline, 6 months ]
    whole dexa body scan to assess bone density with Z scores (more negative z score indicates increased risk for fractures)

  10. Lean Mass % [ Time Frame: Baseline, 6 months ]
    whole body dexa scans to assess lean mass % (0- 100 %). Increase lean mass % is the desired outcome.

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   18 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  1. Patients with Becker muscular dystrophy or LGMD2A (CAPN3), LGMD 2B (DYSF), LGMD 2C (SGCG), LGMD2E (SGCB), LGMD2F (SGCD), LGMD 2I (FKRP), LGMD (ANO5). Genetic mutation or muscle biopsy staining required to confirm genetic subtype
  2. Ages 18-65 years
  3. EKG without evidence of prior infarct or atrial fibrillation done within 2 months of study initiation.
  4. Echocardiogram with LVEF >25% done within 6 months of study initiation.
  5. Stable medications (same medication and dose) for the previous 3 months
  6. Stable pulmonary status for the previous 6 months (No change in FVC by more than 20% in the past 6-months)

Exclusion Criteria:

  1. Diabetes
  2. BMI>35 kg/m2
  3. Cardiac transplantation
  4. Myocardia Infarct in the past 2-years from screening
  5. Any history of tuberculosis
  6. Untreated or uncontrolled (medication and/or dose change in previous month from screening) hypertension
  7. A diagnosis of congestive heart failure
  8. A diagnosis of chronic kidney disease
  9. A diagnosis of untreated hypothyroidism
  10. The patient is believed to be at high risk of osteoporosis by the primary investigator
  11. Inability to provide consent
  12. Full time ventilator dependency
  13. Heart failure symptoms or LVEF <25%
  14. Orthopedic surgery within the prior year or upcoming elective orthopedic surgery within the 6-months from Day 0.
  15. Inability to complete MRI (claustrophobia, metal implants)
  16. Pregnant women at screening, women seeking to become pregnant, or men seeking to father a child within 6-months from Day 0 should not participate in this study.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04054375

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United States, Illinois
Northwestern University
Chicago, Illinois, United States, 60611
Sponsors and Collaborators
Northwestern University
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Principal Investigator: Senda Ajroud-Driss, MD Associate Professor of Neurology (Neuromuscular Disease)
  Study Documents (Full-Text)

Documents provided by Senda Ajroud-Driss, Northwestern University:
Study Protocol  [PDF] August 12, 2019
No Statistical Analysis Plan (SAP) exists for this study.


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Responsible Party: Senda Ajroud-Driss, Associate Professor of Neurology (Neuromuscular Disease), Northwestern University
ClinicalTrials.gov Identifier: NCT04054375    
Other Study ID Numbers: STU00208443
First Posted: August 13, 2019    Key Record Dates
Results First Posted: July 8, 2021
Last Update Posted: February 16, 2023
Last Verified: January 2023
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Product Manufactured in and Exported from the U.S.: No
Keywords provided by Senda Ajroud-Driss, Northwestern University:
Steroids, Prednisone
Additional relevant MeSH terms:
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Muscular Dystrophies
Muscular Dystrophy, Duchenne
Muscular Dystrophies, Limb-Girdle
Muscular Disorders, Atrophic
Muscular Diseases
Musculoskeletal Diseases
Neuromuscular Diseases
Nervous System Diseases
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Anti-Inflammatory Agents
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs
Antineoplastic Agents, Hormonal
Antineoplastic Agents